跳至主要内容
临床试验/CTRI/2018/10/015943
CTRI/2018/10/015943已完成未知

COMPARATIVE STUDY TO ASSESS THE EFFICACY AND COSTEFFICIENCY OF IMMUNOLOGICALLY- TARGETED LOW DOSERITUXIMAB PROTOCOL WITH THE CONVENTIONALRHEUMATOID ARTHRITIS PROTOCOL IN SIGNIFICANT PEMPHIGUS

DEPARTMENT OF DERMATOLOGY0 个研究点目标入组 23 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
23

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • PATIENTS OF PEMPHIGUS VULGARIS OR PEMPHIGUS FOLIACEOUS IN THE ABOVE MENTIONED AGE GROUP WITH SIGNIFICANT CLINICAL DISEASE WITH PDAI( PEMPHIGUS DISEASE ACTIVITY INDEX) SCORE >15 AND WHO ARE WILLING FOR MONTHLY FOLLOW UP VISITS FOR 12 MONTHS.

排除标准

  • PATIENTS WITH ACTIVE OR LATENT INFECTIONS LIKE HEPATITIS, TB OR SEPSIS.PREGNANT AND LACTATING FEMALES, PATIENTS WITH KNOWN CARDIAC ABNORMALITIES OR ARRHYTHMIA, SEVERELY DECREASED BONE MARROW FUNCTIONS, KNOWN HYPERSENSITIVITY TO MURINE PROTEINS OR ORAL CORTICOSTEROIDS. PATIENTS WHO HAVE RECEIVED RITUXIMAB IN PRECEDING 12 MONTHS OR DEXAMETHASONE PULSE THERAPY IN PRECEDING 3 MONTHS WILL ALSO BE EXCLUDED.

研究者

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